Call Us:IRL +353 (0)61-335844 / UK +44 (0)28 30833808

IVD

  • Internal Quality Control Software from Technopath Manufacturing Ltd. IAMQC Daily is a comprehensive Internal Quality Control software that applies Westgard and/or any user-defined QC rules to individual QC results. The software automatically builds interactive Levey-Jennings charts and tables and provides summary and detailed customised reports to the end user. IAMQC Daily integrates with Microsoft Excel to produce customised electronic reports. The system also allows the import of pre-defined templates, resulting in instant system setups. Users can create audit trails, action logs and summary reports at the click of a button. IAMQC Daily comprises a centralised program that facilitates the analysis of multiple QC materials, across numerous departments in a laboratory setting. The system can also be integrated with IAMQC Peer to satisfy both Internal and External QC requirements. IAMQC Daily offers a centralised review of all QC data from all laboratories/instruments. Central administrator access facilitates managers to review QC performance at multiple facilities – no need to visit each laboratory site. Closer monitoring of QC from remote locations without additional costs provides a flexible option for managing the inter and intra-lab performance. The software works on an ‘open’ platform that allows the end user to add all types of control material from a range of laboratories. Both IAMQC Daily and Expert can run using an internet OR intranet connection. Each PC license allows the user to manage an unlimited number of departments, control materials (not limited to Technopath materials) and instruments. An unlimited number of user logins can be added to the system at any stage. An administrator module can also manage user logins, customising the functionality that is available to each user. All data can also be filtered using the same logic to apply a user-friendly atmosphere and save time scrolling through data.
  • Select QC Rules and make meaningful QC decisions IAMQC Expert, from Technopath Manufacturing Ltd, is an interactive system that helps front line laboratory staff select QC rules, reduce unnecessary repeats and make meaningful QC decisions. IAMQC Expert allows the end-user to monitor method performance relative to clinical requirements and focus on the tests that require their attention. Times and technologies are changing rapidly. Instruments and methodologies are more accurate, precise and stable than they were a decade ago. Most laboratories have adopted these new technical advances, but few have modified their QC processes to match. Many laboratories are still using a 1-2s rule as recommended by Levey and Jennings in 1951. Technopath Manufacturing Ltd  have designed a QC system that will alert users to significant changes and not generate QC flags when the system is operating safely within acceptable limits. The system compares method performance to defined quality requirements (rather than to last month’s data) and recommends QC strategies that will warn users when QC data points exceed acceptable performance - with a minimal number of false flags. In the design of our QC system we “balance” the quality control system to meet the changing performance and stability of the analytical system.
  • Innovative, real-time, Peer Comparison Software from Technopath Manufacturing Ltd. The web based system facilitates laboratories testing the same lot number of control material to access valuable information from their colleagues through peer comparison. The reports that are generated in IAMQC Peer compare the accuracy and precision of analytical processes between laboratories and peer groups. This information can be extremely valuable, indicating the user’s performance relative to their peer group and also providing powerful troubleshooting tools when attempting to resolve potential problems. To participate in IAMQC Peer, each individual laboratory submits their individual results or summary statistics (mean, standard deviation, and number of data points) to the central database maintained by Technopath Manufacturing Ltd. Laboratories data may be submitted manually on-line or, alternatively, captured by one of our many interfacing options. The information provided by IAMQC Peer can be used on a monthly basis to evaluate how well lab’s methods are operating, relative to the overall peer group. Users can also look at this peer data in real-time, interactive, tables online, when they are investigating a potential problem with accuracy or precision for an individual method.
  • Immunohaematology Methods for Manual Techniques
    Manual Techniques from Diagast Historically, hemagglutination methods are performed with liquid reagents on slide, opaline plates or tube supports. See below for the Diagast manual techniques offering and full list of immunohaematology methods.
  • Diagast Immunohaematology QC
    Precision. Confidence. Compliance. Technopath is proud to partner with Diagast, a global leader in immunohaematology, to deliver a comprehensive range of quality control solutions designed to ensure accuracy, reliability, and full regulatory compliance in transfusion laboratories with ISO 15189 requirements. Diagast’s immunohaematology quality control portfolio supports laboratories in maintaining the highest standards across blood grouping, antibody screening, crossmatching, and reagent performance verification—helping safeguard patient outcomes at every stage of the transfusion pathway. Comprehensive Quality Control for Transfusion Safety In immunohaematology, precision is critical. Diagast’s quality controls are specifically developed to:
    • Monitor assay performance across routine and specialised testing
    • Verify reagent integrity and system functionality
    • Ensure compliance with ISO 15189 and local regulatory standards (HPRA, UKAS)
    • Reduce risk of transfusion errors and improve laboratory confidence
    With robust validation and consistent performance, Diagast QC materials enable laboratories to detect deviations early, maintain consistency, and support accreditation requirements.
  • Morphle MorphoLens 1
    Introducing MorphoLens 1 from Morphle The MorphoLens 1 is a compact, entry-level digital pathology scanner designed for laboratories transitioning to digital workflows. It provides reliable whole slide imaging (WSI) with integrated AI-driven image optimisation and cloud-ready data management. Key Applications:
    • Histopathology (H&E, IHC)
    • Cytology and rapid on-site evaluation
    • Frozen section analysis
    Why Choose MorphoLens 1? Ideal for low-to-medium throughput laboratories, this system offers an accessible entry point into digital pathology, supporting both clinical and research workflows.
  • Morphle MorphoLens 240
    Introducing MorphoLens 240 from Morphle Built for enterprise-scale labs, the MorphoLens 240 offers industrial-level throughput for high-volume histopathology and cancer diagnostics labs. Key Applications:
    • High-volume histopathology labs
    • Cancer diagnostics and screening programmes
    • Centralised digital pathology services
  • Morphle MorphoLens 6
    Introducing MorphoLens 6 from Morphle The MorphoLens 6 is designed for laboratories requiring greater throughput without compromising on flexibility or footprint. With batch scanning and AI-powered quality control, it delivers efficient and consistent digital pathology workflows. Key Applications:
    • Histopathology (H&E, IHC, special stains)
    • Cytology (FNAC, LBC)
    • Mixed laboratory workflows
    Why Choose MorphoLens 6? Optimised for labs processing up to ~100 slides per day, MorphoLens 6 provides a balance of throughput, performance, and affordability
  • Multichem A1c Control, from Technopath Manufacturing Ltd, is intended for use as a third party, bi- level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Haemoglobin A1c determination Assays. The intended patient population are those with diabetes. The haemoglobin A1c test, also called HbA1c, glycated haemoglobin test, or glycol-haemoglobin, is an important blood test that shows how well a patient’s diabetes is being controlled. Multichem A1c Control is designed as a bi-level, liquid stable frozen product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Multichem AE (Ammonia Ethanol) Control, from Technopath Manufacturing Ltd, is intended for use as a third party liquid stable quality control material to monitor the precision of laboratory testing procedures for Ammonia and Ethanol Assays. Multichem AE Control is designed as a liquid stable frozen product. The product will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Anti Mullerian Hormone QC Anti-Müllerian Hormone QC
    Multichem AMH Control, from Technopath Manufacturing Ltd, is intended for use as a third party, tri-level, liquid stable quality control material to monitor the precision of laboratory testing procedures for Anti Mullerian Hormone Assays. The product will typically be run to provide a minimum of 2 levels of control to monitor AMH assay performance within the analytical ranges. Multichem AMH Control will be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The product should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The Control is to be stored at -20°C to –80°C and thawed as per IFU prior to use. The product is to be stored at 2 to 8°C between use.
  • Cerebral Spinal Fluid QC Cerebral Spinal Fluid QC
    Third party, bi-level, liquid stable, multi-analyte quality control material to monitor the precision of laboratory testing procedures for Cerebral Spinal Fluid Assays. Multichem CSF, from Technopath Manufacturing Ltd,  contains 4 analytes including CSF glucose, protein, IgG and lactate. Multichem CSF Controls are designed as bi-level, liquid stable frozen products. These products will typically be run after reagent calibration and at a frequency dictated by laboratory QC procedures and reagent / instrument manufacturer instructions. The products should be treated the same as patient specimens and run in accordance with the instructions accompanying the instrument, kit or reagent being used. The controls are should be stored at -20°C to -80°C and thawed as per IFU prior to use. The products should be stored at 2 to 8°C between use.
Go to Top